Fully Automated Production of 11C-Doxepin for PET Imaging Histamine H1 Receptor

被引:2
作者
Cai, Hancheng [1 ,2 ,3 ]
Mangner, Thomas J. [1 ,3 ]
Muzik, Otto [1 ,2 ,3 ,4 ]
Lu, Xin [1 ,2 ]
Chakraborty, Pulak K. [1 ,3 ]
Chugani, Diane C. [1 ,2 ,3 ]
Chugani, Harry T. [1 ,2 ,3 ,4 ]
机构
[1] Childrens Hosp Michigan, Detroit Med Ctr, PET Ctr, Detroit, MI 48201 USA
[2] Wayne State Univ, Sch Med, Carman & Ann Adams Dept Pediat, Detroit, MI USA
[3] Wayne State Univ, Sch Med, Dept Radiol, Detroit, MI USA
[4] Wayne State Univ, Sch Med, Dept Neurol, Detroit, MI 48201 USA
关键词
C-11; labeling; Doxepin; Radiosynthesis; Histamine H1 receptor; PET; POSITRON-EMISSION-TOMOGRAPHY; H-1; RECEPTOR; HUMAN BRAIN; DOXEPIN; OCCUPANCY; COMPLEX;
D O I
10.1007/s11307-011-0535-x
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
C-11-Doxepin is an established positron emission tomography (PET) probe for imaging the histamine H1 receptor, which is associated with various neurological disorders and allergic diseases. A fully automated current Good Manufacturing Practices (cGMP)-compliant radiosynthesis is therefore desirable in order to facilitate clinical PET studies. We report here a fully automated production method for C-11-doxepin using a multipurpose PET module for clinical use. C-11-Doxepin was radiosynthesized by N-[C-11]methylation of nordoxepin using [C-11]methyl iodide in DMF solvent, and then purified by HPLC, and finally reformulated with solid phase extraction (SPE) using a cGMP-compliant automated multipurpose PET module developed in house. The final product was analyzed and subjected to quality control according to current US Pharmacopeia requirements. The radiochemical yield (decay corrected) of C-11-doxepin for clinical use was 47.0 +/- 5.2% (n = 12) based on [C-11]methyl iodide, moreover the radiochemical purity of C-11-doxepin was more than 97.5% with 1,200 +/- 500 Ci/mmol specific activity(end of production). The total production time of C-11-doxepin was 37 min from end of bombardment (EOB) with the final product passing all tests under cGMP requirements for clinical use. A simplified and reliable fully automated production of (11) C-doxepin for clinical use was developed, allowing the synthesis of the tracer with high yield using a cGMP-compliant module and procedure. The success of this approach could make the PET tracer (11) C-doxepin more accessible for clinical studies.
引用
收藏
页码:546 / 552
页数:7
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